JP3917863B2 - Pde4アイソザイムの選択的阻害薬として有用なニコチンアミドベンゾ縮合複素環誘導体 - Google Patents
Pde4アイソザイムの選択的阻害薬として有用なニコチンアミドベンゾ縮合複素環誘導体 Download PDFInfo
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- JP3917863B2 JP3917863B2 JP2001557868A JP2001557868A JP3917863B2 JP 3917863 B2 JP3917863 B2 JP 3917863B2 JP 2001557868 A JP2001557868 A JP 2001557868A JP 2001557868 A JP2001557868 A JP 2001557868A JP 3917863 B2 JP3917863 B2 JP 3917863B2
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- Prior art keywords
- formula
- methyl
- nicotinamide
- benzo
- oxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- YLVAGBJBSYSJJJ-UHFFFAOYSA-N CC(C(C(c(cc1)ccc1SC)=O)N1)NC1=O Chemical compound CC(C(C(c(cc1)ccc1SC)=O)N1)NC1=O YLVAGBJBSYSJJJ-UHFFFAOYSA-N 0.000 description 1
- GRNSAEXUTAGBSL-UHFFFAOYSA-N CC(C)(c1ccc(CN(CC=C)CC=C)cc1)O Chemical compound CC(C)(c1ccc(CN(CC=C)CC=C)cc1)O GRNSAEXUTAGBSL-UHFFFAOYSA-N 0.000 description 1
- NDHOQAPKKVXVEH-UHFFFAOYSA-N CC(C)C(C(C)C)C(c(cc1OC)ccc1OCCCCCOc(cc1)ccc1C(N)=N)=O Chemical compound CC(C)C(C(C)C)C(c(cc1OC)ccc1OCCCCCOc(cc1)ccc1C(N)=N)=O NDHOQAPKKVXVEH-UHFFFAOYSA-N 0.000 description 1
- NPFVRBCDMFKOPY-UHFFFAOYSA-N CC(C1)C(c2cc(-[n]3cncc3)c[s]2)=NNC1=O Chemical compound CC(C1)C(c2cc(-[n]3cncc3)c[s]2)=NNC1=O NPFVRBCDMFKOPY-UHFFFAOYSA-N 0.000 description 1
- BEIZIEZPGSIQGR-UHFFFAOYSA-N CS(Nc1ccc(Oc(cc2)ccc2F)[s]1)(=O)=O Chemical compound CS(Nc1ccc(Oc(cc2)ccc2F)[s]1)(=O)=O BEIZIEZPGSIQGR-UHFFFAOYSA-N 0.000 description 1
- YEEZWCHGZNKEEK-UHFFFAOYSA-N Cc(cccc1)c1S(NC(c1cc(OC)c(Cc(c2c3)c[n](C)c2ccc3NC(OC2CCCC2)=O)cc1)=O)(=O)=O Chemical compound Cc(cccc1)c1S(NC(c1cc(OC)c(Cc(c2c3)c[n](C)c2ccc3NC(OC2CCCC2)=O)cc1)=O)(=O)=O YEEZWCHGZNKEEK-UHFFFAOYSA-N 0.000 description 1
- ZGSYVUBKPBUTDW-UHFFFAOYSA-N NCc1ccc(C2(CC2)O)cc1 Chemical compound NCc1ccc(C2(CC2)O)cc1 ZGSYVUBKPBUTDW-UHFFFAOYSA-N 0.000 description 1
- DABPGEIBZBRJFL-UHFFFAOYSA-N OC(c(cccn1)c1Oc1cc2n[s]nc2cc1)=O Chemical compound OC(c(cccn1)c1Oc1cc2n[s]nc2cc1)=O DABPGEIBZBRJFL-UHFFFAOYSA-N 0.000 description 1
- 0 [*+]c1ccc(*)[s]1 Chemical compound [*+]c1ccc(*)[s]1 0.000 description 1
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- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
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- Immunology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Psychiatry (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17928400P | 2000-01-31 | 2000-01-31 | |
| US60/179,284 | 2000-01-31 | ||
| PCT/IB2001/000124 WO2001057036A1 (fr) | 2000-01-31 | 2001-01-30 | Derives benzocondenses heterocycliques de nicotinamide utiles comme inhibiteurs selectifs d'isozymes pde4 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003522176A JP2003522176A (ja) | 2003-07-22 |
| JP3917863B2 true JP3917863B2 (ja) | 2007-05-23 |
Family
ID=22655931
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001557868A Expired - Fee Related JP3917863B2 (ja) | 2000-01-31 | 2001-01-30 | Pde4アイソザイムの選択的阻害薬として有用なニコチンアミドベンゾ縮合複素環誘導体 |
Country Status (41)
| Country | Link |
|---|---|
| US (1) | US7354941B2 (fr) |
| EP (1) | EP1252158B1 (fr) |
| JP (1) | JP3917863B2 (fr) |
| KR (1) | KR20020072299A (fr) |
| CN (1) | CN1404481A (fr) |
| AP (1) | AP2002002589A0 (fr) |
| AR (1) | AR027337A1 (fr) |
| AT (1) | ATE293624T1 (fr) |
| AU (1) | AU2700201A (fr) |
| BG (1) | BG106852A (fr) |
| BR (1) | BR0107964A (fr) |
| CA (1) | CA2398182C (fr) |
| CO (1) | CO5261634A1 (fr) |
| CZ (1) | CZ20022410A3 (fr) |
| DE (1) | DE60110205T2 (fr) |
| EA (1) | EA004885B1 (fr) |
| EE (1) | EE200200425A (fr) |
| ES (1) | ES2238415T3 (fr) |
| GE (1) | GEP20043302B (fr) |
| GT (1) | GT200100022A (fr) |
| HN (1) | HN2001000019A (fr) |
| HU (1) | HUP0204262A2 (fr) |
| IL (1) | IL150641A0 (fr) |
| IS (1) | IS6421A (fr) |
| MA (1) | MA26870A1 (fr) |
| MX (1) | MXPA02007419A (fr) |
| NO (1) | NO20023613L (fr) |
| NZ (1) | NZ519547A (fr) |
| OA (1) | OA12169A (fr) |
| PA (1) | PA8511201A1 (fr) |
| PE (1) | PE20011058A1 (fr) |
| PL (1) | PL357995A1 (fr) |
| PT (1) | PT1252158E (fr) |
| PY (1) | PY0102109A (fr) |
| SK (1) | SK10142002A3 (fr) |
| SV (1) | SV2002000299A (fr) |
| TN (1) | TNSN01020A1 (fr) |
| TR (1) | TR200201880T2 (fr) |
| UY (1) | UY26569A1 (fr) |
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| ZA (1) | ZA200206033B (fr) |
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| EP1322614A2 (fr) | 2000-09-18 | 2003-07-02 | E. I. du Pont de Nemours and Company | Pyridinyl-amides et pyridinyl-imides utilis s comme fongicides |
| EE200300360A (et) | 2001-01-31 | 2003-12-15 | Pfizer Products Inc. | PDE4 isosüümide inhibiitoritena kasutatavad nikotiinamiidi biarüülderivaadid |
| ES2248231T3 (es) * | 2001-01-31 | 2006-03-16 | Pfizer Products Inc. | Derivados de eteres utiles como inhibidores de las isozimas pde4. |
| CN1489588A (zh) | 2001-01-31 | 2004-04-14 | �Ʒ� | 用作pde4同功酶抑制剂的噻唑基,噁唑基,吡咯基,和咪唑基羧酸酰胺衍生物 |
| US7250518B2 (en) | 2001-01-31 | 2007-07-31 | Pfizer Inc. | Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes |
| GB0118373D0 (en) * | 2001-07-27 | 2001-09-19 | Glaxo Group Ltd | Novel therapeutic method |
| JP2005505570A (ja) * | 2001-09-19 | 2005-02-24 | アルタナ ファルマ アクチエンゲゼルシャフト | Pde阻害剤及びロイコトリエン受容体拮抗物質の複合薬 |
| US20040242597A1 (en) * | 2001-09-19 | 2004-12-02 | Thomas Klein | Combination |
| IS7221A (is) * | 2001-11-15 | 2004-04-15 | Memory Pharmaceuticals Corporation | Hringlaga adenosínmónófosfat fosfódíesterasa 4D7 ísóform og aðferðir til notkunar þeirra |
| MXPA04007737A (es) | 2002-02-11 | 2004-10-15 | Pfizer | Derivados de nicotinamida utiles como inhibidores de fosfodesterasas 4. |
| US6756392B2 (en) | 2002-02-11 | 2004-06-29 | Pfizer Inc | Nicotinamide derivatives useful as PDE4 inhibitors |
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| WO2004047817A1 (fr) * | 2002-11-27 | 2004-06-10 | Altana Pharma Ag | Inhibiteurs de pde4 et pde3/4 que l'on utilise dans le traitement de la cachexie |
| AU2003300076C1 (en) | 2002-12-30 | 2010-03-04 | Angiotech International Ag | Drug delivery from rapid gelling polymer composition |
| JPWO2004087151A1 (ja) * | 2003-03-31 | 2006-06-29 | 協和醗酵工業株式会社 | 医薬組成物 |
| WO2004087150A1 (fr) * | 2003-03-31 | 2004-10-14 | Kyowa Hakko Kogyo Co. Ltd. | Composition pour medicaments |
| US20060199789A1 (en) * | 2003-03-31 | 2006-09-07 | Kyowa Hakko Kogyo Co., Ltd. | medical composition |
| EP1616024A1 (fr) * | 2003-04-10 | 2006-01-18 | F. Hoffmann-La Roche Ag | Utilisation de pde4d dans le criblage de medicaments contre l'atherosclerose |
| WO2004104022A2 (fr) * | 2003-05-16 | 2004-12-02 | The General Hospital Corporation | Compositions contenant un facteur chimio-tactique epithelial pathogene (eicosanoide et hepoxiline a3), leurs inhibiteurs et leurs procedes d'utilisation |
| GB0317516D0 (en) | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Nicotinamide derivatives useful as PDE4 inhibitors |
| GB0317498D0 (en) * | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Compounds |
| GB0317484D0 (en) | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Nicotinamide derivatives useful as pde4 inhibitors |
| GB0317471D0 (en) * | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Novel compounds |
| US7153870B2 (en) | 2003-07-25 | 2006-12-26 | Pfizer Inc. | Nicotinamide derivatives useful as PDE4 inhibitors |
| US7132435B2 (en) | 2003-07-25 | 2006-11-07 | Pfizer Inc. | Compounds |
| PE20060272A1 (es) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a |
| EP1683795A1 (fr) * | 2005-01-21 | 2006-07-26 | Pfizer Limited | Formes crystallines de cis-5-fluoro-N-¬4-(2-hydroxy-4-methylbenzamido)cyclohexyl|-2-(tetrahydrothiopyran-4-yloxy)nicotinamide |
| EP1844040A1 (fr) * | 2005-01-21 | 2007-10-17 | Pfizer Limited | Formes crystallines de cis-5-fluoro-n-[4-(2-hydroxy-4-methylbenzamido)cyclohexyl]-2-(tetrahydrothiopyran-4-yloxy)nicotinamide |
| GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
| GB0624282D0 (en) * | 2006-12-05 | 2007-01-10 | Cavalla David | Treatment of cachexia |
| WO2008079328A2 (fr) * | 2006-12-22 | 2008-07-03 | Creighton University | Acides gras oméga-5 utiles dans l'inhibition de la 5-lipoxygénase et dans le traitement du cancer |
| KR20100014565A (ko) * | 2007-04-11 | 2010-02-10 | 알콘 리서치, 리미티드 | 알레르기성 비염 및 알레르기성 결막염을 치료하기 위한 tnfa의 억제제 및 항히스타민의 용도 |
| EP2196465A1 (fr) | 2008-12-15 | 2010-06-16 | Almirall, S.A. | Dérivés de (3-oxo)pyridazin-4-ylurée comme inhibiteurs de PDE4 |
| EP2226323A1 (fr) | 2009-02-27 | 2010-09-08 | Almirall, S.A. | Nouveaux dérivés de tétrahydropyrazolo [3,4-c]isoquinoléine-5-amine |
| USRE46608E1 (en) | 2009-09-01 | 2017-11-14 | Catabasis Pharmaceuticals, Inc. | Fatty acid niacin conjugates and their uses |
| WO2011028689A1 (fr) | 2009-09-01 | 2011-03-10 | Catabasis Pharmaceuticals, Inc. | Conjugués acides gras niacine et leurs utilisations |
| EP2380890A1 (fr) | 2010-04-23 | 2011-10-26 | Almirall, S.A. | Nouveaux dérivés de 7,8-dihydro-1,6-naphthyridin-5(6h)-one comme PDE4 inhibiteurs |
| EP2386555A1 (fr) * | 2010-05-13 | 2011-11-16 | Almirall, S.A. | Nouveaux dérivés de cyclohéxylamine dotés d'activités agoniste bêta 2 adrénergique et antagoniste muscarinique m3 |
| EP2394998A1 (fr) | 2010-05-31 | 2011-12-14 | Almirall, S.A. | Dérivés de 3-(5-Amino-6-oxo-1,6-dihydropyridazin-3-yl)-biphenyl en tant qu'inhibiteurs de la PDE4 |
| EP3270929B1 (fr) * | 2015-03-17 | 2019-09-11 | Lee, Sheau-Long | Utilisation de ginsenoside m1 pour la prévention ou le traitement de la silicose |
| US11116737B1 (en) | 2020-04-10 | 2021-09-14 | University Of Georgia Research Foundation, Inc. | Methods of using probenecid for treatment of coronavirus infections |
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| US4861891A (en) * | 1988-08-31 | 1989-08-29 | Pfizer Inc. | Antidepressant N-substituted nicotinamide compounds |
| TW429148B (en) | 1995-10-27 | 2001-04-11 | Pfizer | Pharmaceutical agents for the treatment of acute and chronic inflammatory diseases |
| AU738037B2 (en) | 1997-04-04 | 2001-09-06 | Pfizer Products Inc. | Nicotinamide derivatives |
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